Evidence map›Paper›PMID 25031744›Full record

ArticleInternational journal of clinical and experimental pathology2014

Concurrent CD44s and STAT3 expression in human clear cell renal cellular carcinoma and its impact on survival.

Jun Qin, Bo Yang, Bao-Qin Xu, Amber Smithc, Liang Xu, Jian-Lin Yuan, Ling Li

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Renal Cell Carcinoma: Molecular Aspects.Indian journal of clinical biochemistry : IJCB · 2018
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Jun QinDepartment of Urology, Xijing Hospital, Fourth Military Medical University 15 West Changle Street, Xi'an, Shaanxi 710032, China.
Bo YangDepartment of Urology, Xijing Hospital, Fourth Military Medical University 15 West Changle Street, Xi'an, Shaanxi 710032, China.
Bao-Qin XuDepartment of Cell Biology and Cell Engineering Research Centre, State Key Laboratory of Cancer Biology, Fourth Military Medical University 17 West Changle Street, Xi'an, Shaanxi 710032, China.
Amber SmithcDepartments of Molecular Biosciences, Radiation Oncology and Urology, University of Kansas 1200 Sunnyside Avenue, Lawrence, KS 66045, USA.
Liang XuDepartments of Molecular Biosciences, Radiation Oncology and Urology, University of Kansas 1200 Sunnyside Avenue, Lawrence, KS 66045, USA.
Jian-Lin YuanDepartment of Urology, Xijing Hospital, Fourth Military Medical University 15 West Changle Street, Xi'an, Shaanxi 710032, China.
Ling LiDepartment of Cell Biology and Cell Engineering Research Centre, State Key Laboratory of Cancer Biology, Fourth Military Medical University 17 West Changle Street, Xi'an, Shaanxi 710032, China.
Xijing Hospital · CNAir Force Medical University · CNUniversity of Kansas · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although CD44 was overexpressed and considered as a useful prognostic marker in renal cell carcinoma, the prognostic role of CD44s in clear cell renal cell carcinoma (ccRCC) remains controversial. Moreover, the correlation and prognostic significance of CD44s and its downstream signaling target pSTAT3 are unclear in ccRCC. In this study, 75 pairs of carcinoma and paired adjacent non-tumor renal tissue samples were collected from patients with localized ccRCC who underwent a nephrectomy. The expression levels of CD44s and pSTAT3 were analyzed using immunohistochemistry. Correlations between CD44s/pSTAT3 expression and clinical and pathological characteristics were determined using x(2) test, Kaplan-Meier analysis and Cox's proportional hazards model. We found that CD44s is highly expressed in 46.67% of tumor tissues, and its high expression was significantly associated with high tumor grade (P < 0.001), large tumor size (P = 0.009) and advanced T stage (P = 0.004). A strong correlation exists between high expression of CD44s and pSTAT3 (r = 0.4013, P = 0.0004). The joint over expression of CD44s and pSTAT3 was present in 42.66% of tumor specimens and had an additive negative impact on overall survival. Patients with CD44s(high)pSTAT3(high) expression had significantly poor survival as compared to patients with CD44s(low)pSTAT3(low) tumor expression (P = 0.024), though the concurrent overexpression of CD44s and pSTAT3 was not an independent prognostic factor for overall survival. Our data indicate that expression of both CD44s and pSTAT3 in ccRCC is associated with advanced tumor stage and patient survival. The conclusions from this study may improve the prediction of ccRCC prognosis information when CD44s and pSTAT3 expression are evaluated together with classical clinicopathological parameters.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCarcinoma, Renal CellFemaleHumansHyaluronan ReceptorsImmunohistochemistryKaplan-Meier EstimateKidney NeoplasmsMaleMiddle AgedPrognosisProportional Hazards ModelsSTAT3 Transcription FactorBiomarkers, TumorCD44 protein, humanHyaluronan ReceptorsSTAT3 protein, humanSTAT3 Transcription FactorccRCCCD44sprognosispSTAT3survival

Identifiers

PMID25031744
PMCPMC4097256
OpenAlexW56544914

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.